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Development of CDK4/6 Inhibitors: A Five Years Update

The inhibition of cyclin dependent kinases 4 and 6 plays a role in aromatase inhibitor resistant metastatic breast cancer. Three dual CDK4/6 inhibitors have been approved for the breast cancer treatment that, in combination with the endocrine therapy, dramatically improved the survival outcomes both...

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Autores principales: Ammazzalorso, Alessandra, Agamennone, Mariangela, De Filippis, Barbara, Fantacuzzi, Marialuigia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7967197/
https://www.ncbi.nlm.nih.gov/pubmed/33803309
http://dx.doi.org/10.3390/molecules26051488
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author Ammazzalorso, Alessandra
Agamennone, Mariangela
De Filippis, Barbara
Fantacuzzi, Marialuigia
author_facet Ammazzalorso, Alessandra
Agamennone, Mariangela
De Filippis, Barbara
Fantacuzzi, Marialuigia
author_sort Ammazzalorso, Alessandra
collection PubMed
description The inhibition of cyclin dependent kinases 4 and 6 plays a role in aromatase inhibitor resistant metastatic breast cancer. Three dual CDK4/6 inhibitors have been approved for the breast cancer treatment that, in combination with the endocrine therapy, dramatically improved the survival outcomes both in first and later line settings. The developments of the last five years in the search for new selective CDK4/6 inhibitors with increased selectivity, treatment efficacy, and reduced adverse effects are reviewed, considering the small-molecule inhibitors and proteolysis-targeting chimeras (PROTACs) approaches, mainly pointing at structure-activity relationships, selectivity against different kinases and antiproliferative activity.
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spelling pubmed-79671972021-03-18 Development of CDK4/6 Inhibitors: A Five Years Update Ammazzalorso, Alessandra Agamennone, Mariangela De Filippis, Barbara Fantacuzzi, Marialuigia Molecules Review The inhibition of cyclin dependent kinases 4 and 6 plays a role in aromatase inhibitor resistant metastatic breast cancer. Three dual CDK4/6 inhibitors have been approved for the breast cancer treatment that, in combination with the endocrine therapy, dramatically improved the survival outcomes both in first and later line settings. The developments of the last five years in the search for new selective CDK4/6 inhibitors with increased selectivity, treatment efficacy, and reduced adverse effects are reviewed, considering the small-molecule inhibitors and proteolysis-targeting chimeras (PROTACs) approaches, mainly pointing at structure-activity relationships, selectivity against different kinases and antiproliferative activity. MDPI 2021-03-09 /pmc/articles/PMC7967197/ /pubmed/33803309 http://dx.doi.org/10.3390/molecules26051488 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ammazzalorso, Alessandra
Agamennone, Mariangela
De Filippis, Barbara
Fantacuzzi, Marialuigia
Development of CDK4/6 Inhibitors: A Five Years Update
title Development of CDK4/6 Inhibitors: A Five Years Update
title_full Development of CDK4/6 Inhibitors: A Five Years Update
title_fullStr Development of CDK4/6 Inhibitors: A Five Years Update
title_full_unstemmed Development of CDK4/6 Inhibitors: A Five Years Update
title_short Development of CDK4/6 Inhibitors: A Five Years Update
title_sort development of cdk4/6 inhibitors: a five years update
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7967197/
https://www.ncbi.nlm.nih.gov/pubmed/33803309
http://dx.doi.org/10.3390/molecules26051488
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